FDA recall record

Karoun Dairies Braided String Cheese with Natural Hickory Smoke Jumbo Braided recall — FDA F-0091-2016

Karoun Dairies is recalling all cheese manufactured from an identified manufacturer due to potential Listeria monocytogenes contamination.

Class Iclassification
F-0091-2016official record ID
Oct 28, 2015report date

Recall record at a glance

Official recordF-0091-2016
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmKaroun Dairies
Report dateOct 28, 2015
Recall initiation dateSep 16, 2015
Quantity1.6 million lbs (total all cheese)
LocationSan Fernando, CA, United States

Official product description

Braided String Cheese with Natural Hickory Smoke Jumbo Braided String Cheese with Natural Hickory Smoke 5oz, 8lb UPC Codes: 96252 00019 5, 7 96252 00020 1, 7 96252 00035 5, 7 96252 00015 7, 7 96252 00025 6, 7 96252 00041 6, 7 96252 00042 3, 7 96252 00040 9, 7 96252 00005 8, 7 96252 00008 9, 7 96252 00038 6, 7 96252 00028 7, 7 96252 00018 8, 7 96252 00013 3, 7 96252 00017 1, 7 96252 00016 4, 7 96252 00039 3, 7 96252 00022 5 Product is vacuum packed, packaged in plastic containers, or packed on styrofoam trays wrapped in plastic.

Why the product was recalled

Karoun Dairies is recalling all cheese manufactured from an identified manufacturer due to potential Listeria monocytogenes contamination.

Distribution information

U.S. distribution nationwide. Foreign distribution to the following; Canada and Malaysia

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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